Iron‐catalyzed  tandem reactions  of aldehydes, terminal alkynes, and primary amines as a strategy for the synthesis of quinoline derivatives | Zendy

Zhang Yicheng | Zendy; Li Pinhua | Zendy; Wang Lei | Zendy

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Iron‐catalyzed tandem reactions of aldehydes, terminal alkynes, and primary amines as a strategy for the synthesis of quinoline derivatives

Author(s) -

Zhang Yicheng,

Li Pinhua,

Wang Lei

Publication year - 2011

Publication title -

journal of heterocyclic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.321

H-Index - 59

eISSN - 1943-5193

pISSN - 0022-152X

DOI - 10.1002/jhet.417

Subject(s) - chemistry , quinoline , tandem , primary (astronomy) , catalysis , combinatorial chemistry , organic chemistry , condensation , aldehyde , materials science , physics , astronomy , composite material , thermodynamics

FeCl 3 ‐catalyzed three‐component tandem condensation/addition/cyclization/oxidation reactions of aldehydes, terminal alkynes, and primary amines have been developed. The processes can provide a diverse range of quinoline derivatives in good yields from simple starting materials. A possible reaction mechanism was proposed. J. Heterocyclic Chem., (2010).

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